52092-27-0 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
(2-phenylcyclohexyl)acetic acid is utilized as a chiral building block for the synthesis of various pharmaceuticals and agrochemicals, playing a crucial role in the development of new drugs and agricultural products.
Used in Anti-inflammatory and Analgesic Applications:
(2-phenylcyclohexyl)acetic acid is employed as a potential anti-inflammatory and analgesic agent, due to its capacity to modulate inflammatory responses and provide pain relief.
Used in Neurodegenerative Disease Treatment:
(2-phenylcyclohexyl)acetic acid is studied for its potential role in the treatment of neurodegenerative diseases, suggesting that it may offer neuroprotective benefits.
Used in Cancer Treatment Research:
(2-phenylcyclohexyl)acetic acid is also being investigated for its potential contribution to cancer treatment, indicating a possible role in managing or treating cancerous conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 52092-27-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,0,9 and 2 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 52092-27:
(7*5)+(6*2)+(5*0)+(4*9)+(3*2)+(2*2)+(1*7)=100
100 % 10 = 0
So 52092-27-0 is a valid CAS Registry Number.
52092-27-0Relevant academic research and scientific papers
Conformational Effects in the Hydrolyses of Rigid Benzylic Epoxides: Implications for Diol Epoxides of Polycyclic Hydrocarbons
Sayer, J. M.,Yagi, H.,Silverton, J. V.,Friedman, S. L.,Whalen, D. L.,Jerina, D. M.
, p. 1972 - 1978 (2007/10/02)
The two conformationally rigid, diastereomeric 9,10-oxides derived from trans-1,2,3,4,4a,10a-hexahydrophenanthrene have been synthesized, and their relative stereochemistries have been verified by X-ray structure determination of the acetate of the bromoh
PHOTOCHEMISTRY OF N-ACYLAZOLES. VI). PHOTOREACTIVITIES OF 1-ACYL-1,2,4-TRIAZOLES AND OF 2-ACYLTETRAZOLES
Murato, Kazuo,Yatsunami, Takashi,Iwasaki, Shigeo
, p. 588 - 605 (2007/10/02)
Contrary to the findings in the photolysis of N-acylimidazoles (2) irradiation of 1-acyl-1,2,4-triazoles afforded no photo-Fries product, but instead products formed via the corresponding acyl radicals and aldehydes.Photolysis of 2-acyltetrazoles gave in part the same products as those obtained from the irradiation of the corresponding acyl-triazoles as well as 2-alkyl-1,3,4-oxadiazoles.N-Acyltetrazoles didn't give any photo-Fries product neither.
